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Cloning and characterization of F3PYC gene encoding pyruvate carboxylase in Aspergillus flavus strain (F3)
Pyruvate carboxylase is a major enzyme for biosynthesis of organic acids like; citric acid, fumeric acid, and l -malic acid. These organic acids play very important role for biological remediation of heavy metals. In this study, gene walking method was used to clone and characterize pyruvate carboxy...
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Published in: | 3 Biotech 2017-08, Vol.7 (4), p.245-245, Article 245 |
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description | Pyruvate carboxylase is a major enzyme for biosynthesis of organic acids like; citric acid, fumeric acid, and
l
-malic acid. These organic acids play very important role for biological remediation of heavy metals. In this study, gene walking method was used to clone and characterize pyruvate carboxylase gene (
F3PYC)
from heavy metal resistant indigenous fungal isolate
Aspergillus flavus
(F3). 3579 bp of an open reading frame which encodes 1193 amino acid protein (isoelectric point: 6.10) with a calculated molecular weight of 131.2008 kDa was characterized. Deduced protein showed 90–95% similarity to those deduced from
PYC
gene from different fungal strains including;
Aspergillus parasiticus
,
Neosartorya fischeri
,
Aspergillus fumigatus
,
Aspergillus clavatus,
and
Aspergillus niger
. Protein generated from the
PYC
gene was a homotetramer (α4) and having four potential N-linked glycosylation sites and had no signal peptide. Amongst most possible N-glycosylation sites were –N–S–S–I– at 36 amino acid, –N–G–T–V– at 237 amino acid, N–G–S–S– at 517 amino acid, and N–T–S–R– at 1111 amino acid, with several functions have been proposed for the carbohydrate moiety such as thermal stability, pH, and temperature optima for activity and stabilization of the three-dimensional structure. Hence, cloning of
F3PYC
gene from
A. flavus
has important biotechnological applications. |
doi_str_mv | 10.1007/s13205-017-0806-6 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5511116</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1920197042</sourcerecordid><originalsourceid>FETCH-LOGICAL-c503t-8e1442db35690588ed17588f7add992464681690a49a835df24dcb0507b53a523</originalsourceid><addsrcrecordid>eNqFkU-L1DAYxoMo7rLuB_AiAS_rofomTZr0IiyDo8KCHhT0FNI07WbIJGPSDjt-elNmHf-AmMsbeH558iQPQk8JvCQA4lUmNQVeAREVSGiq5gE6p6SFiotaPjzt6ZczdJnzBsrihLcEHqMzKgUBwdg52qx8DC6MWIcem1udtJlsct_15GLAccDr-uPXFR5tsNgGE_uF3R3SvNeTxUanLt4dvM4Wu4Cv886m0Xk_Zzx4vS8jT0kX5Wpdv3iCHg3aZ3t5Py_Q5_WbT6t31c2Ht-9X1zeV4VBPlbSEMdp3NW9a4FLanogyBqH7vm0pa1gjSZE0a7WseT9Q1psOOIiO15rT-gK9Pvru5m5re2NDyeDVLrmtTgcVtVN_KsHdqjHuFeekrKYYXN0bpPhttnlSW5eN9V4HG-esKFCQggnG_4uSlgJpBbAl1vO_0E2cUyg_UQxLg6QYskKRI2VSzDnZ4ZSbgFp6V8feVeldLb2rJe-z3x98OvGz5QLQI5CLFEabfl39b9cfhku3Dg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2008014744</pqid></control><display><type>article</type><title>Cloning and characterization of F3PYC gene encoding pyruvate carboxylase in Aspergillus flavus strain (F3)</title><source>Springer Nature</source><source>PubMed Central</source><creator>Qayyum, Sadia ; Khan, Ibrar ; Bhatti, Zulfiqar Ahmad ; Peng, Changsheng</creator><creatorcontrib>Qayyum, Sadia ; Khan, Ibrar ; Bhatti, Zulfiqar Ahmad ; Peng, Changsheng</creatorcontrib><description>Pyruvate carboxylase is a major enzyme for biosynthesis of organic acids like; citric acid, fumeric acid, and
l
-malic acid. These organic acids play very important role for biological remediation of heavy metals. In this study, gene walking method was used to clone and characterize pyruvate carboxylase gene (
F3PYC)
from heavy metal resistant indigenous fungal isolate
Aspergillus flavus
(F3). 3579 bp of an open reading frame which encodes 1193 amino acid protein (isoelectric point: 6.10) with a calculated molecular weight of 131.2008 kDa was characterized. Deduced protein showed 90–95% similarity to those deduced from
PYC
gene from different fungal strains including;
Aspergillus parasiticus
,
Neosartorya fischeri
,
Aspergillus fumigatus
,
Aspergillus clavatus,
and
Aspergillus niger
. Protein generated from the
PYC
gene was a homotetramer (α4) and having four potential N-linked glycosylation sites and had no signal peptide. Amongst most possible N-glycosylation sites were –N–S–S–I– at 36 amino acid, –N–G–T–V– at 237 amino acid, N–G–S–S– at 517 amino acid, and N–T–S–R– at 1111 amino acid, with several functions have been proposed for the carbohydrate moiety such as thermal stability, pH, and temperature optima for activity and stabilization of the three-dimensional structure. Hence, cloning of
F3PYC
gene from
A. flavus
has important biotechnological applications.</description><identifier>ISSN: 2190-572X</identifier><identifier>EISSN: 2190-5738</identifier><identifier>DOI: 10.1007/s13205-017-0806-6</identifier><identifier>PMID: 28710744</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Agriculture ; Amino acids ; Aspergillus clavatus ; Aspergillus fischeri ; Aspergillus flavus ; Aspergillus fumigatus ; Aspergillus niger ; Aspergillus parasiticus ; Bioinformatics ; Biomaterials ; Biosynthesis ; Biotechnology ; Cancer Research ; Carbohydrates ; Chemistry ; Chemistry and Materials Science ; Citric acid ; Cloning ; Fungi ; genes ; genome walking ; Glycosylation ; Heavy metals ; isoelectric point ; Malic acid ; moieties ; Molecular weight ; open reading frames ; Organic acids ; Original ; Original Article ; Proteins ; Pyc gene ; Pyruvate carboxylase ; Pyruvic acid ; remediation ; signal peptide ; Stem Cells ; temperature ; Thermal stability</subject><ispartof>3 Biotech, 2017-08, Vol.7 (4), p.245-245, Article 245</ispartof><rights>Springer-Verlag GmbH Germany 2017</rights><rights>3 Biotech is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-8e1442db35690588ed17588f7add992464681690a49a835df24dcb0507b53a523</citedby><cites>FETCH-LOGICAL-c503t-8e1442db35690588ed17588f7add992464681690a49a835df24dcb0507b53a523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511116/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511116/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27898,27899,53763,53765</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28710744$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qayyum, Sadia</creatorcontrib><creatorcontrib>Khan, Ibrar</creatorcontrib><creatorcontrib>Bhatti, Zulfiqar Ahmad</creatorcontrib><creatorcontrib>Peng, Changsheng</creatorcontrib><title>Cloning and characterization of F3PYC gene encoding pyruvate carboxylase in Aspergillus flavus strain (F3)</title><title>3 Biotech</title><addtitle>3 Biotech</addtitle><addtitle>3 Biotech</addtitle><description>Pyruvate carboxylase is a major enzyme for biosynthesis of organic acids like; citric acid, fumeric acid, and
l
-malic acid. These organic acids play very important role for biological remediation of heavy metals. In this study, gene walking method was used to clone and characterize pyruvate carboxylase gene (
F3PYC)
from heavy metal resistant indigenous fungal isolate
Aspergillus flavus
(F3). 3579 bp of an open reading frame which encodes 1193 amino acid protein (isoelectric point: 6.10) with a calculated molecular weight of 131.2008 kDa was characterized. Deduced protein showed 90–95% similarity to those deduced from
PYC
gene from different fungal strains including;
Aspergillus parasiticus
,
Neosartorya fischeri
,
Aspergillus fumigatus
,
Aspergillus clavatus,
and
Aspergillus niger
. Protein generated from the
PYC
gene was a homotetramer (α4) and having four potential N-linked glycosylation sites and had no signal peptide. Amongst most possible N-glycosylation sites were –N–S–S–I– at 36 amino acid, –N–G–T–V– at 237 amino acid, N–G–S–S– at 517 amino acid, and N–T–S–R– at 1111 amino acid, with several functions have been proposed for the carbohydrate moiety such as thermal stability, pH, and temperature optima for activity and stabilization of the three-dimensional structure. Hence, cloning of
F3PYC
gene from
A. flavus
has important biotechnological applications.</description><subject>Agriculture</subject><subject>Amino acids</subject><subject>Aspergillus clavatus</subject><subject>Aspergillus fischeri</subject><subject>Aspergillus flavus</subject><subject>Aspergillus fumigatus</subject><subject>Aspergillus niger</subject><subject>Aspergillus parasiticus</subject><subject>Bioinformatics</subject><subject>Biomaterials</subject><subject>Biosynthesis</subject><subject>Biotechnology</subject><subject>Cancer Research</subject><subject>Carbohydrates</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Citric acid</subject><subject>Cloning</subject><subject>Fungi</subject><subject>genes</subject><subject>genome walking</subject><subject>Glycosylation</subject><subject>Heavy metals</subject><subject>isoelectric point</subject><subject>Malic acid</subject><subject>moieties</subject><subject>Molecular weight</subject><subject>open reading frames</subject><subject>Organic acids</subject><subject>Original</subject><subject>Original Article</subject><subject>Proteins</subject><subject>Pyc gene</subject><subject>Pyruvate carboxylase</subject><subject>Pyruvic acid</subject><subject>remediation</subject><subject>signal peptide</subject><subject>Stem Cells</subject><subject>temperature</subject><subject>Thermal stability</subject><issn>2190-572X</issn><issn>2190-5738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkU-L1DAYxoMo7rLuB_AiAS_rofomTZr0IiyDo8KCHhT0FNI07WbIJGPSDjt-elNmHf-AmMsbeH558iQPQk8JvCQA4lUmNQVeAREVSGiq5gE6p6SFiotaPjzt6ZczdJnzBsrihLcEHqMzKgUBwdg52qx8DC6MWIcem1udtJlsct_15GLAccDr-uPXFR5tsNgGE_uF3R3SvNeTxUanLt4dvM4Wu4Cv886m0Xk_Zzx4vS8jT0kX5Wpdv3iCHg3aZ3t5Py_Q5_WbT6t31c2Ht-9X1zeV4VBPlbSEMdp3NW9a4FLanogyBqH7vm0pa1gjSZE0a7WseT9Q1psOOIiO15rT-gK9Pvru5m5re2NDyeDVLrmtTgcVtVN_KsHdqjHuFeekrKYYXN0bpPhttnlSW5eN9V4HG-esKFCQggnG_4uSlgJpBbAl1vO_0E2cUyg_UQxLg6QYskKRI2VSzDnZ4ZSbgFp6V8feVeldLb2rJe-z3x98OvGz5QLQI5CLFEabfl39b9cfhku3Dg</recordid><startdate>201708</startdate><enddate>201708</enddate><creator>Qayyum, Sadia</creator><creator>Khan, Ibrar</creator><creator>Bhatti, Zulfiqar Ahmad</creator><creator>Peng, Changsheng</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>LK8</scope><scope>M7P</scope><scope>M7S</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>201708</creationdate><title>Cloning and characterization of F3PYC gene encoding pyruvate carboxylase in Aspergillus flavus strain (F3)</title><author>Qayyum, Sadia ; Khan, Ibrar ; Bhatti, Zulfiqar Ahmad ; Peng, Changsheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-8e1442db35690588ed17588f7add992464681690a49a835df24dcb0507b53a523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Agriculture</topic><topic>Amino acids</topic><topic>Aspergillus clavatus</topic><topic>Aspergillus fischeri</topic><topic>Aspergillus flavus</topic><topic>Aspergillus fumigatus</topic><topic>Aspergillus niger</topic><topic>Aspergillus parasiticus</topic><topic>Bioinformatics</topic><topic>Biomaterials</topic><topic>Biosynthesis</topic><topic>Biotechnology</topic><topic>Cancer Research</topic><topic>Carbohydrates</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Citric acid</topic><topic>Cloning</topic><topic>Fungi</topic><topic>genes</topic><topic>genome walking</topic><topic>Glycosylation</topic><topic>Heavy metals</topic><topic>isoelectric point</topic><topic>Malic acid</topic><topic>moieties</topic><topic>Molecular weight</topic><topic>open reading frames</topic><topic>Organic acids</topic><topic>Original</topic><topic>Original Article</topic><topic>Proteins</topic><topic>Pyc gene</topic><topic>Pyruvate carboxylase</topic><topic>Pyruvic acid</topic><topic>remediation</topic><topic>signal peptide</topic><topic>Stem Cells</topic><topic>temperature</topic><topic>Thermal stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qayyum, Sadia</creatorcontrib><creatorcontrib>Khan, Ibrar</creatorcontrib><creatorcontrib>Bhatti, Zulfiqar Ahmad</creatorcontrib><creatorcontrib>Peng, Changsheng</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>3 Biotech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qayyum, Sadia</au><au>Khan, Ibrar</au><au>Bhatti, Zulfiqar Ahmad</au><au>Peng, Changsheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning and characterization of F3PYC gene encoding pyruvate carboxylase in Aspergillus flavus strain (F3)</atitle><jtitle>3 Biotech</jtitle><stitle>3 Biotech</stitle><addtitle>3 Biotech</addtitle><date>2017-08</date><risdate>2017</risdate><volume>7</volume><issue>4</issue><spage>245</spage><epage>245</epage><pages>245-245</pages><artnum>245</artnum><issn>2190-572X</issn><eissn>2190-5738</eissn><abstract>Pyruvate carboxylase is a major enzyme for biosynthesis of organic acids like; citric acid, fumeric acid, and
l
-malic acid. These organic acids play very important role for biological remediation of heavy metals. In this study, gene walking method was used to clone and characterize pyruvate carboxylase gene (
F3PYC)
from heavy metal resistant indigenous fungal isolate
Aspergillus flavus
(F3). 3579 bp of an open reading frame which encodes 1193 amino acid protein (isoelectric point: 6.10) with a calculated molecular weight of 131.2008 kDa was characterized. Deduced protein showed 90–95% similarity to those deduced from
PYC
gene from different fungal strains including;
Aspergillus parasiticus
,
Neosartorya fischeri
,
Aspergillus fumigatus
,
Aspergillus clavatus,
and
Aspergillus niger
. Protein generated from the
PYC
gene was a homotetramer (α4) and having four potential N-linked glycosylation sites and had no signal peptide. Amongst most possible N-glycosylation sites were –N–S–S–I– at 36 amino acid, –N–G–T–V– at 237 amino acid, N–G–S–S– at 517 amino acid, and N–T–S–R– at 1111 amino acid, with several functions have been proposed for the carbohydrate moiety such as thermal stability, pH, and temperature optima for activity and stabilization of the three-dimensional structure. Hence, cloning of
F3PYC
gene from
A. flavus
has important biotechnological applications.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28710744</pmid><doi>10.1007/s13205-017-0806-6</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agriculture Amino acids Aspergillus clavatus Aspergillus fischeri Aspergillus flavus Aspergillus fumigatus Aspergillus niger Aspergillus parasiticus Bioinformatics Biomaterials Biosynthesis Biotechnology Cancer Research Carbohydrates Chemistry Chemistry and Materials Science Citric acid Cloning Fungi genes genome walking Glycosylation Heavy metals isoelectric point Malic acid moieties Molecular weight open reading frames Organic acids Original Original Article Proteins Pyc gene Pyruvate carboxylase Pyruvic acid remediation signal peptide Stem Cells temperature Thermal stability |
title | Cloning and characterization of F3PYC gene encoding pyruvate carboxylase in Aspergillus flavus strain (F3) |
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